Self-Compassion, Health, and Empowerment

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorYang Li

About this trial

Intimate partner violence (IPV) can have serious and lasting effects on women's mental health and well-being. Chinese immigrant women in the United States often face additional barriers to obtaining IPV and mental health support, including language, cultural, and social challenges. There is a need for culturally appropriate interventions that improve access to care and address the mental health needs of this underserved population.

The purpose of this study is to evaluate the efficacy of the Self-Compassion, Health, and Empowerment (SHE) intervention, a culturally tailored mobile health (mHealth) program designed for Chinese immigrant women experiencing IPV. Participants will be randomly assigned to either the SHE intervention or an attention control program and will complete study assessments over a 12-month follow-up period.

The results of this study will help determine whether the SHE intervention improves mental health and well-being among Chinese immigrant women experiencing IPV and may provide evidence for an accessible, culturally appropriate intervention that can be implemented more broadly.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age 18 or older;

Self-identify as a woman;

Self-identify as Chinese;

Reside in the U.S.;

Disqualifiers

Those who cannot speak or understand Mandarin or English;

Those with substance use, suicidality, or who have been in mental health care for severe mental illness.

Trial design

Design model

Parallel

Treatments tested in this trial

  • The Self-Compassion, Health, and Empowerment (SHE) Intervention

    Behavioral

    The intervention will consist of 6 weekly sessions. Session 1 is a phone discussion about an IPV safety brochure covering IPV information, questions from the Danger Assessment, safety planning, options, and available resources. It also includes immigrant-specific content such as immigration-related abuse, legal options for immigrants, and resources for immigrant survivors. Sessions 2-6 will focus on providing mental health self-care resources, with a specific topic assigned each week (Deep Breathing, Progressive Muscle Relaxation, Mindful Self- Compassion, Mindfulness, and Loving-Kindness). Each session includes a video introduction on 1 of our 5 topics, with accompanying audio instructions for exercises. The interventionist will guide participants to review the video at the beginning of each session and encourage them to practice the exercises presented in that session daily for 1 week.

  • Health and Nutrition Program

    Behavioral

    It consists of six weekly educational sessions focused on nutrition and health. Each week, participants will view a video on a specific nutrition-related topic and complete a quiz/homework (e.g., food label identification, healthy meal planning). Reminder and check-in messages will be sent every other day via text messages to reinforce the content and respond to any participant questions.

Treatment groups

364 Participants
are divided into 2 treatment groups
Group A: The SHE intervention groupExperimental treatment 1 intervention
Group B: The attention control groupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Depression symptoms

The instrument used will be the Patient Health Questionnaire-9. The total scores range from 0 to 27, with higher scores indicating more severe depressive symptoms.

Time frame
Baseline and 6-week, 3-month, 6-month, and 12-month follow-ups
2

Anxiety symptoms

The instrument used will be the Generalized Anxiety Disorder-7. The total scores range from 0 to 21, with higher scores indicating more severe anxiety symptoms.

Time frame
Baseline and 6-week, 3-month, 6-month, and 12-month follow-ups
3

Symptoms of post-traumatic stress disorder (PTSD)

The instrument used will be the PTSD Checklist for DSM-5. The total scores range from 0 to 80, with higher scores indicating more severe PTSD symptoms.

Time frame
Baseline and 6-week, 3-month, 6-month, and 12-month follow-ups

Secondary outcomes

1

Intimate partner violence

The instrument used will be the Revised Conflict Tactics Scales. Item scores within each subscale were summed, with higher scores indicating more frequent experiences of the corresponding behaviors. The scale consists of five subscales: negotiation (6 items; score range = 0-150), psychological aggression (8 items; score range = 0-200), physical assault (12 items; score range = 0-300), sexual coercion (7 items; score range = 0-175), and injury (6 items; score range = 0-150).

Time frame
Baseline and 6-week, 3-month, 6-month, and 12-month follow-ups

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Yang Li

Lead sponsor

University of Texas at Austin

Sponsor institution

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